Journal
BREAST CANCER RESEARCH
Volume 22, Issue 1, Pages -Publisher
BMC
DOI: 10.1186/s13058-020-01301-x
Keywords
Triple-negative breast cancer; ERK; Akt; Fluorescence microscopy; Mitochondrial fission; Mitochondrial fusion; Metastasis
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Funding
- NIH [R01CA238042, R01CA196018, U01CA210152, R01CA238023, R33CA225549, R50CA221807, R37CA222563]
- American Cancer Society-Michigan Cancer Research Fund Postdoctoral Fellowship [PF-18-236-01-CCG]
- National Science Foundation Graduate Research Fellowship [DGE 1256260]
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Background Mitochondrial dynamics underlies malignant transformation, cancer progression, and response to treatment. Current research presents conflicting evidence for functions of mitochondrial fission and fusion in tumor progression. Here, we investigated how mitochondrial fission and fusion states regulate underlying processes of cancer progression and metastasis in triple-negative breast cancer (TNBC). Methods We enforced mitochondrial fission and fusion states through chemical or genetic approaches and measured migration and invasion of TNBC cells in 2D and 3D in vitro models. We also utilized kinase translocation reporters (KTRs) to identify single cell effects of mitochondrial state on signaling cascades, PI3K/Akt/mTOR and Ras/Raf/MEK/ERK, commonly activated in TNBC. Furthermore, we determined effects of fission and fusion states on metastasis, bone destruction, and signaling in mouse models of breast cancer. Results Enforcing mitochondrial fission through chemical or genetic approaches inhibited migration, invasion, and metastasis in TNBC. Breast cancer cells with predominantly fissioned mitochondria exhibited reduced activation of Akt and ERK both in vitro and in mouse models of breast cancer. Treatment with leflunomide, a potent activator of mitochondrial fusion proteins, overcame inhibitory effects of fission on migration, signaling, and metastasis. Mining existing datasets for breast cancer revealed that increased expression of genes associated with mitochondrial fission correlated with improved survival in human breast cancer. Conclusions In TNBC, mitochondrial fission inhibits cellular processes and signaling pathways associated with cancer progression and metastasis. These data suggest that therapies driving mitochondrial fission may benefit patients with breast cancer.
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